Isleem Raghda S, Eid Ahmed M, Hassan Saad El-Din, Aboshanab Khaled M, El-Housseiny Ghadir S
Department of Microbiology and Immunology, Faculty of Pharmacy, Ain Shams University, Cairo, 11566, Egypt.
Department of Botany and Microbiology, Faculty of Science, Al-Azhar University, Cairo, 11884, Egypt.
AMB Express. 2025 Jan 13;15(1):10. doi: 10.1186/s13568-024-01811-3.
In this study, Allium sativum, garlic, was selected to isolate endophytic bacteria and to evaluate the antimicrobial, antiviral, antioxidant, and cytotoxic activities of their produced metabolites followed by identification of the biosynthetic gene cluster of the antimicrobial metabolites using Oxford Nanopore Technology (ONT). Two bacterial isolates, C6 and C11, were found to have a broad-spectrum antagonistic effect against four standard microbial strains and were molecularly identified using 16 S ribosomal RNA sequence analysis and deposited in a local culture collection as B. velezensis CCASU-C6, and B. subtilis CCASU-C11, respectively. Optimization for the maximum production of antimicrobial metabolites revealed that a four-day incubation period was optimal, with sucrose and tryptone serving as the best carbon and nitrogen sources for the fermentation media. Response surface methodology model using the central composite design was created resulting in a 1.2-fold and 1.8-fold improvement in antimicrobial metabolite(s) production of C6 and C11 isolates, respectively. The optimal production conditions were found to be a temperature of 33 °C, pH of 7, and an agitation rate of 200 rpm for C6 metabolite, and a temperature of 37 °C, pH of 7, and an agitation rate of 250 rpm for C11 metabolite. Both bacterial isolates displayed antioxidant and antiviral activity and mild cytotoxic action. Genomic sequence and antiSMASH analysis showed that the biosynthetic gene clusters of bacillomycin, mycosubtilin, fengycin, and macrolactin H in B. velezensis CCASU-C6 and bacillibactin and Macrolactin H in B. subtilis CCASU-C11 showed 100% conservation.
在本研究中,选择大蒜(葱属植物)来分离内生细菌,并评估其产生的代谢产物的抗菌、抗病毒、抗氧化和细胞毒性活性,随后使用牛津纳米孔技术(ONT)鉴定抗菌代谢产物的生物合成基因簇。发现两株细菌分离株C6和C11对四种标准微生物菌株具有广谱拮抗作用,并通过16S核糖体RNA序列分析进行分子鉴定,分别作为贝莱斯芽孢杆菌CCASU - C6和枯草芽孢杆菌CCASU - C11保藏于当地的菌种保藏库。抗菌代谢产物最大产量的优化表明,四天的培养期是最佳的,蔗糖和胰蛋白胨分别是发酵培养基的最佳碳源和氮源。使用中心复合设计创建了响应面方法模型,使C6和C11分离株的抗菌代谢产物产量分别提高了1.2倍和1.8倍。发现C6代谢产物的最佳生产条件为温度33℃、pH值7和搅拌速度200 rpm,C11代谢产物的最佳生产条件为温度37℃、pH值7和搅拌速度250 rpm。两株细菌分离株均表现出抗氧化和抗病毒活性以及轻微的细胞毒性作用。基因组序列和antiSMASH分析表明,贝莱斯芽孢杆菌CCASU - C6中的杆菌霉素、真菌枯草菌素、丰原素和大环内酯H以及枯草芽孢杆菌CCASU - C11中的杆菌铁载体和大环内酯H的生物合成基因簇具有100%的保守性。